Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR891B (microRNA 891b)

Identity

Alias_namesMIRN891B
Alias_symbol (synonym)hsa-mir-891b
Other alias
HGNC (Hugo) MIR891B
LocusID (NCBI) 100126304
Atlas_Id 70299
Location Xq27.3  [Link to chromosome band Xq27]
Location_base_pair Starts at 146001053 and ends at 146001131 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)MIR891B   33645
Cards
Entrez_Gene (NCBI)MIR891B  100126304  microRNA 891b
AliasesMIRN891B
GeneCards (Weizmann)MIR891B
Ensembl hg19 (Hinxton)ENSG00000216064 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000216064 [Gene_View]  chrX:146001053-146001131 [Contig_View]  MIR891B [Vega]
ICGC DataPortalENSG00000216064
TCGA cBioPortalMIR891B
AceView (NCBI)MIR891B
Genatlas (Paris)MIR891B
WikiGenes100126304
SOURCE (Princeton)MIR891B
Genetics Home Reference (NIH)MIR891B
miRBaseMIR891B
dbDEMCMIR891B
Genomic and cartography
GoldenPath hg38 (UCSC)MIR891B  -     chrX:146001053-146001131 -  Xq27.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR891B  -     Xq27.3   [Description]    (hg19-Feb_2009)
EnsemblMIR891B - Xq27.3 [CytoView hg19]  MIR891B - Xq27.3 [CytoView hg38]
Mapping of homologs : NCBIMIR891B [Mapview hg19]  MIR891B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR891B
Alternative Splicing GalleryENSG00000216064
Gene ExpressionMIR891B [ NCBI-GEO ]   MIR891B [ EBI - ARRAY_EXPRESS ]   MIR891B [ SEEK ]   MIR891B [ MEM ]
Gene Expression Viewer (FireBrowse)MIR891B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100126304
GTEX Portal (Tissue expression)MIR891B
Human Protein AtlasENSG00000216064-MIR891B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR891B
DMDM Disease mutations100126304
Blocks (Seattle)MIR891B
Human Protein Atlas [tissue]ENSG00000216064-MIR891B [tissue]
Protein Interaction databases
FunCoupENSG00000216064
BioGRIDMIR891B
STRING (EMBL)MIR891B
ZODIACMIR891B
Ontologies - Pathways
Huge Navigator MIR891B [HugePedia]
snp3D : Map Gene to Disease100126304
BioCentury BCIQMIR891B
ClinGenMIR891B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100126304
Chemical/Pharm GKB GenePA164722992
Clinical trialMIR891B
Miscellaneous
canSAR (ICR)MIR891B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR891B
EVEXMIR891B
GoPubMedMIR891B
iHOPMIR891B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Nov 9 12:17:20 CET 2017

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